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letter
. 2020 Jul 7;67:109977. doi: 10.1016/j.jclinane.2020.109977

Safe percutaneous dilational tracheostomy in 5 patients with ARDS by Covid-19

Manuel Taboada 1,2,, Sara Vazquez 1,2, Julia Regueira 1,2, Agustín Cariñena 1,2, Francisco Aneiros 1,2, Valentin Caruezo 1,2, Alberto Naveira 1,2, Pablo Otero 1,2
PMCID: PMC7340012  PMID: 32653759

To the Editor:

Coronavirus disease 2019 (Covid-19), caused by the novel severe acute respiratory syndrome coronavirus (SARS-CoV-2), is a disease with a clinical spectrum that ranges from asymptomatic to critical disease requiring Intensive Care Unit (ICU) admission, intubation, and prolonged mechanical ventilation due to a severe acute respiratory distress syndrome (ARDS) [1]. Despite the large and growing number of cases of Covid-19 disease around the world, there are few publications related to the performance of tracheostomies in Covid-19 patients who require prolonged mechanical ventilation. We describe our experience in 5 patients with laboratory-confirmed COVID-19 admitted in the ICU of Clinical Hospital of Santiago de Compostela who underwent elective bedside percutaneous dilational tracheostomies (PDT) during April 2020. This prospective case series was approved by the Research Ethics Committee of the Galicia, Spain, number 2020-188. Informed consent for the procedure was provided by all patients or a close relative of the patient. All patients were admitted with severe ARDS. Patient demographics, comorbidities, clinical ICU course and treatments are described in Table 1 . Tracheostomy was performed after a mean of 16 (13-27) days of invasive mechanical ventilation and the patients presented a PaO2/FiO2 ratio of 167 (92-206). PTD took place in ICU, in a closed room. Team that performed PTD consisted of 3 anesthesiologists and a circulation nurse. One anesthesiologist managed airway and bronchoscopy, and the other two performed the PTD. Each person wore standard personal protective equipment PPE (FFP3 mask, surgical cap, goggles, surgical gown, and double gloves). During procedure, all patients were deep sedated and paralyzed. During tracheal puncture mechanical ventilation was stopped and we used a Single-Step dilatation technique (Ciaglia Blue Rhino G2 Advanced Percutaneous Tracheostomy Kit (Cook Medical)) with the help of a bronchoscope to control the puncture site, the direction of guidewire, and the location of tracheostomy. PTD was performed at the bedside in all five patients without difficulty, and no complications were found. Neither the nurse nor the anesthetists who participated in the PTD developed symptoms or tested positive for Covid-19 fourteen days after procedure.

Table 1.

Clinical Characteristics patients with severe ARDS by COVID-19 where tracheostomy was performed.

Patient 1 Patient 2 Patient 3 Patient 4 Patient 5
Characteristics
 Age, yr 68 70 70 63 68
 Sex, F M M M M
 Weight, kg 65 92 75 90 97
 Height, cm 165 165 162 176 166
 APACHE II score 21 17 21 16 20
 PaO2/FiO2 in ICU admission (mmHg) 180 206 92 133 173
 PaO2 in ICU admission (mmHg) 80 124 92 106 104
 Chronic medical illness
 Hypertension No Yes Yes No Yes
 Diabetes No No No No Yes
 Chronic obstructive pulmonary disease Yes No No No No
 Heart disease No Yes Si No Yes
 Laboratory parameters
 Leukocytes count per mL 17980 8400 4800 3450 7400
 Lymphocytes count per mL 230 510 180 280 1080
 C-reactive protein, mg/L 25 15 5 7 17
 D-dimer, ng/mL 4870 707 1900 357 1295
 Lactate dehydrogenase, U/L 989 600 248 519 913
 Creatine kinase, ng/mL 291 140 33 110 54
 Serum Ferritin, μg/L 531 2650 689 2898 653
 Interleukin-6, pg/mL 158 85 1819 670 77
 Procalcitonin, ng/mL 13,3 0,32 64 0,46 0,22
 Triglycerides, mg/dL 127 195 118 256 117
 Treatment
 Hydroxychloroquine Yes Yes Yes Yes Yes
 Lopinavir/ritonavir Yes Yes Yes Yes Yes
 Azithromycin Yes Yes Yes Yes Yes
 Tocilizumab No No Yes No Yes
 Glucocorticoids Yes Yes Yes Yes Yes
Clinical ICU course
 Duration since intubation to tracheostomy (days) 13 27 17 16 16
 Length of ICU stay (days) 39 31 38 40 39a
 Survival at 21 after PTD Yes Yes No No Yes
a

Remained ICU, PTD: percutaneous dilational tracheostomies.

PTD is a common, minimally invasive procedure to facilitate tracheostomy placement, and it represents an alternative to traditional open tracheostomy. We prefer to perform PTD because it is fast, safe, and with low complications. It is performed in our ICU at bedside, avoiding transport of Covid-19 patients to the operating room with repeated connection and disconnection of ventilatory circuits during transfer. Although open tracheostomies were favored over PTD during the SARS outbreak [2], techniques for PTD have advanced since then. We used a single stage “Rhino” dilator technique avoiding multiple entries. Procedure was performed under deep sedation and full neuromuscular blockade to prevent coughing, and we stopped mechanical ventilation just before performing the PTD, to minimize aerosol generation. Although the use of the bronchoscope could generate an increase in aerosols, we believe that it is worth using it due to the increased safety for the patient when performing the procedure. During the procedure we paid meticulous attention to the details of infection control, to minimize cross-contamination and our risk of contracting the illness [3,4].

The optimal timing of tracheostomy in ventilated Covid-19 patients remains controversial. We perform our PTD 14 days after endotracheal intubation (IOT) as recommends the American of Otolaryngology-Head and Neck surgery [5].

In conclusion, there is no evidence whether PTD or surgical open tracheotomy is less aerosol generating. We considered that PTD may be a safe and effective technique for COVID-19 patients with ARDS. Future studies will determine the role of percutaneous tracheostomy in Covid-19 patients with difficult disconnection from mechanical ventilation.

Clinical trial number: Code No. 2020-188.

Prior presentations

No.

Funding statement

No funding provided.

Support

Support was provided solely from institutional and departmental sources.

Authors contributions

  • 1.

    Conception of the study: Manuel Taboada, Valentin Caruezo

  • 2.

    Study design: Manuel Taboada,

  • 3.

    Data collection: Manuel Taboada, Agustín Cariñena, Francisco Aneiros, Albero Naveira, Pablo Otero.

  • 4.

    Data analysis: Manuel Taboada

  • 5.

    Drafting the manuscript: All authors helped to revise the draft of the manuscript

  • 6.

    Editing and approval of the manuscript: All authors

Declaration of competing interest

The authors declare the absence of conflict of interests.

Acknowledgments

The authors thank all physicians and nurses of the Hospital Clínico Universitario Santiago de Compostela. Spain.

References

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Articles from Journal of Clinical Anesthesia are provided here courtesy of Elsevier

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